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Results: 1 to 20 of 62

References for PMC Articles for PubMed (Select 18481271)

1.

Analyses of data on rates of cytogenetic disorders in live births.

Hook EB, Hamerton JL.

Am J Hum Genet. 1978 May;30(3):330-1. No abstract available.

3.

Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY.

Visootsak J, Rosner B, Dykens E, Tartaglia N, Graham JM Jr.

Am J Med Genet A. 2007 Jun 1;143A(11):1198-203.

PMID:
17497714
4.

Male pubertal development and the role of androgen therapy.

Richmond EJ, Rogol AD.

Nat Clin Pract Endocrinol Metab. 2007 Apr;3(4):338-44. Review.

PMID:
17377616
5.

Essential tremor: emerging views of a common disorder.

Benito-León J, Louis ED.

Nat Clin Pract Neurol. 2006 Dec;2(12):666-78; quiz 2p following 691. Review.

PMID:
17117170
6.

Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy.

Shaffer BL, Caughey AB, Norton ME.

Prenat Diagn. 2006 Aug;26(8):667-71.

PMID:
16724363
7.

Cancer incidence and mortality in men with Klinefelter syndrome: a cohort study.

Swerdlow AJ, Schoemaker MJ, Higgins CD, Wright AF, Jacobs PA; UK Clinical Cytogenetics Group.

J Natl Cancer Inst. 2005 Aug 17;97(16):1204-10.

8.

Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.

Zinn AR, Ramos P, Elder FF, Kowal K, Samango-Sprouse C, Ross JL.

J Clin Endocrinol Metab. 2005 Sep;90(9):5041-6. Epub 2005 Jun 14.

PMID:
15956082
10.

Essential tremor among children.

Jankovic J, Madisetty J, Vuong KD.

Pediatrics. 2004 Nov;114(5):1203-5.

PMID:
15520096
11.

Colobomas of the iris and choroid and high signal intensity cerebral foci on T2-weighted magnetic resonance images in Klinefelter's syndrome.

Boettger MB, Kirchhof K, Sergi C, Sakmann C, Meyer P.

J Pediatr Ophthalmol Strabismus. 2004 Jul-Aug;41(4):247-8.

PMID:
15305539
12.

Expression of SHOX in human fetal and childhood growth plate.

Munns CJ, Haase HR, Crowther LM, Hayes MT, Blaschke R, Rappold G, Glass IA, Batch JA.

J Clin Endocrinol Metab. 2004 Aug;89(8):4130-5.

PMID:
15292358
13.

Two 48,XXYY patients: clinical, cytogenetic and molecular aspects.

Zelante L, Piemontese MR, Francioli G, Calvano S.

Ann Genet. 2003 Oct-Dec;46(4):479-81.

PMID:
14659786
14.

Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome.

Kirsch S, Weiss B, Zumbach K, Rappold G.

Hum Genet. 2004 Jan;114(2):173-81. Epub 2003 Oct 25.

PMID:
14579146
15.

AN XXYY VARIANT OF THE KLINEFELTER SYNDROME IN A PREPUBERTAL BODY.

TOWNES PL, ZIEGLER NA, SCHEINER AP.

J Pediatr. 1965 Sep;67:410-4. No abstract available.

PMID:
14339399
16.

STUDIES ON A BOY WITH XXYY CHROMOSOME CONSTITUTION.

SCHLEGEL RJ, ASPILLAGA MJ, NEU R, GARDNER LI.

Pediatrics. 1965 Jul;36:113-9. No abstract available.

PMID:
14313354
17.

TWO CASES OF (PREPUBERTAL) KLINEFELTER'S SYNDROME WITH XXYY SEX CHROMOSOMES.

LEISTI JT, AULA PP, HJELT LH.

Ann Hum Genet. 1964 Sep;28:71-6. No abstract available.

PMID:
14204853
18.

KLINEFELTER'S SYNDROME WITH THE XXYY SEX CHROMOSOME COMPLEX. WITH PARTICULAR REFERENCE TO PREPUBERTAL DIAGNOSIS.

ROBINSON GC, MILLER JR, DILL FJ, KAMBUROFF TD.

J Pediatr. 1964 Aug;65:226-32. No abstract available.

PMID:
14198413
19.

KLINEFELTER'S SYNDROME DUE TO XXYY CHROMOSOME ANOMALY.

TABATA T, FEDOROFF S, GERRARD JW.

Can Med Assoc J. 1964 Feb 29;90:590-2. No abstract available.

20.

THE XXYY VARIANT OF KLINEFELTER'S SYNDROME.

BARR ML, CARR DH, SOLTAN HC, WIENS RG, PLUNKETT ER.

Can Med Assoc J. 1964 Feb 29;90:575-80.

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